Online Directory

Section 1A

Disorders MIM Genes MIM Specialties Commissioning
Pachyonychia Congenita 1; PC1 167200
keratin 16; KRT16 148067
keratin 6A; KRT6A 148041
  • Clinical Genetics
Pachyonychia Congenita 2; PC2 167210
keratin 17; KRT17 148069
keratin 6B; KRT6B 148042
  • Clinical Genetics
Pallister-Hall Syndrome; PHS 146510
GLI family zinc finger 3; GLI3 165240
  • Clinical Genetics
  • Endocrinology, Paediatric
  • Neurology, Paediatric
  • Paediatrics
Palmoplantar Keratoderma, Epidermolytic; EPPK 144200
keratin 1; KRT1 139350
keratin 9; KRT9 607606
  • Dermatology, Adult
  • Dermatology, Paediatric
Pancreatic And Cerebellar Agenesis; PACA 609069
pancreas specific transcription factor, 1A; PTF1A 607194
  • Clinical Genetics
Pancreatitis, Hereditary; PCTT 167800
protease, serine 1; PRSS1 276000
serine peptidase inhibitor, Kazal type 1; SPINK1 167790
  • Clinical Genetics
  • Gastroenterology, Adult
Paragangliomas 1; PGL1 168000
succinate dehydrogenase complex subunit D; SDHD 602690
  • Clinical Genetics
  • Endocrinology, Adult
Paragangliomas 3; PGL3 605373
succinate dehydrogenase complex subunit C; SDHC 602413
  • Clinical Genetics
  • Endocrinology, Adult
Paragangliomas 4; PGL4 115310
succinate dehydrogenase complex iron sulfur subunit B; SDHB 185470
  • Clinical Genetics
  • Endocrinology, Adult
Parietal Foramina 1; PFM1 168500
msh homeobox 2; MSX2 123101
  • Clinical Genetics

Filters

Search filters